Canonical Allele Identifier: CA478869498

Gene: GYS2

Linked Data

• MyVariant Identifiers: chr12:g.21715900T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562966T>C , CM000674.2:g.21562966T>C	GRCh38
NC_000012.11:g.21715900T>C , CM000674.1:g.21715900T>C	GRCh37
NC_000012.10:g.21607167T>C	NCBI36
NG_016167.1:g.46882A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1014A>G MANE Select	ENSP00000261195.2:p.Gly338=
ENST00000647960.1:c.*1016A>G	ENSP00000497202.1:n.*1016A>G
ENST00000648372.1:n.941A>G
ENST00000261195.2:c.1014A>G	ENSP00000261195.2:p.Gly338=
NM_021957.3:c.1014A>G	NP_068776.2:p.Gly338=
XM_005253352.1:c.1014A>G	XP_005253409.1:p.Gly338=
XM_005253354.2:c.795A>G	XP_005253411.1:p.Gly265=
XM_006719062.2:c.1014A>G	XP_006719125.1:p.Gly338=
XM_006719063.2:c.783A>G	XP_006719126.1:p.Gly261=
NM_021957.4:c.1014A>G MANE Select	NP_068776.2:p.Gly338=
XM_006719063.3:c.783A>G	XP_006719126.1:p.Gly261=
XM_017019245.2:c.1014A>G	XP_016874734.1:p.Gly338=
XM_024448960.1:c.1014A>G	XP_024304728.1:p.Gly338=